All news items of Aimee Casey

Under Horizon Europe, the European Commission together with member states and associated countries decided to implement the Rare Diseases Partnership which brings a unique vision [...]

Over 150 members of Endo-ERN gathered at the Amsterdam UMC earlier this month for the annual Endo-ERN General Assembly (GA). The was the first in-person [...]

Today is an exciting day for our EuRRECa colleagues. A project that has been in the works for weeks and the launch date is finally [...]

Diana Kwast-Hoekstra of the Dutch Pituitary Foundation participated in the Eurordis: Rare Disease Week in Brussels. Diana is an Endo-ERN ePAG representative for MTG1. While [...]

The work of Endo-ERN’s ePAGs took them across the Atlantic recently as they attended the International Coalition of Organizations Supporting Endocrine Patients (ICOSEP) meeting in [...]

Endo-ERN in partnership with Endocrine Connections has created a Supplemental for Rare Disease Day 2023. Available online, and as a shareable document, this special collection [...]

Congratulations to Endo-ERN Network Coordinator Professor Alberto Pereira Arias for his inspiring Inaugural Lecture held last month. The topic 2034 considered the possibilities for rare [...]

Rare Disease Day (February 28) is the perfect opportunity to remind your colleagues about your involvement with Endo-ERN. We created an A3 poster that you [...]

The Innovative Health Initiative (IHI) has launched its third call for proposals, featuring topics covering rare diseases and mental health, and addressing challenges such as [...]

At a two-day conference (Dec 1-2, 2022) on clinical research networks (CRNs) for rare diseases the experts from different continents gathered in Paris to increase [...]